Variant report

Variant	rs374129666
Chromosome Location	chr6:11635143-11635144
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763532	chr6:11634722-11641048	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11632600-11635800	Enhancers	Pancreas	Pancrea
2	chr6:11633200-11636600	Weak transcription	Fetal Lung	lung
3	chr6:11633200-11636800	Weak transcription	Gastric	stomach
4	chr6:11633200-11640200	Weak transcription	Aorta	Aorta
5	chr6:11633400-11636800	Weak transcription	Lung	lung
6	chr6:11633600-11636600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:11633600-11637000	Weak transcription	NH-A	brain
8	chr6:11633600-11637200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr6:11633600-11637200	Weak transcription	HSMM	muscle
10	chr6:11633600-11637400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:11633800-11637400	Weak transcription	HSMMtube	muscle
12	chr6:11634200-11635600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:11634400-11635200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr6:11634400-11636600	Weak transcription	Stomach Mucosa	stomach
15	chr6:11634800-11637400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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